1-0458-004 AND nstd173 - dbVar - NCBI

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Number of Variants: 14

Variant Region ID	Type	Number of Variant Calls	Study ID	Organism	Clinical Assertion	Location	Genes in region
nsv4373331	copy number variation	45	nstd173	human		GRCh37 chr4: 34,787,148-34,824,730 , GRCh38.p12 chr4: 34,785,526-34,823,108 , GRCh38.p12 chr4\|NW_003315915.1: 277,855-315,437	LOC105378262
nsv4384091	copy number variation	77	nstd173	human		GRCh37 chr11: 49,710,704-49,746,720 , GRCh38.p12 chr11: 49,689,152-49,725,168 , GRCh38.p12 chr11\|NW_019805495.1: 153,334-179,145	GRM5P1
nsv4376212	copy number variation	5	nstd173	human		GRCh37 chr20: 1,557,177-1,590,244 , GRCh38.p12 chr20: 1,576,531-1,609,598	SIRPB1
nsv4370445	copy number variation	3	nstd173	human		GRCh37 chr6: 124,292,594-124,324,610 , GRCh38.p12 chr6: 123,971,449-124,003,465	NKAIN2
nsv4379737	copy number variation	349	nstd173	human		GRCh37 chr1: 169,216,099-169,241,765 , GRCh38.p12 chr1: 169,246,861-169,272,527	NME7
nsv4373299	copy number variation	1	nstd173	human		GRCh37 chr17: 735,325-788,354 , GRCh38.p12 chr17: 832,085-885,114	NXN
nsv4376456	copy number variation	1782	nstd173	human		GRCh37 chr8: 39,246,772-39,386,964 , GRCh38.p12 chr8: 39,389,253-39,529,445	ADAM5, ADAM3A
nsv4371623	copy number variation	2	nstd173	human		GRCh37 chr2: 188,119,655-188,141,180 , GRCh38.p12 chr2: 187,254,928-187,276,453	CALCRL-AS1, RNU6-989P
nsv4380191	copy number variation	59	nstd173	human		GRCh37 chr1: 1,627,906-1,672,603 , GRCh38.p12 chr1: 1,696,467-1,741,164	MMP23A, LOC100129381, 2 more genes
nsv4368821	copy number variation	1373	nstd173	human		GRCh37 chr22: 24,353,749-24,385,040 , GRCh38.p12 chr22\|NT_187633.1: 247,924-279,215	LOC391322, GSTTP2, 3 more genes
nsv4384905	copy number variation	3	nstd173	human		GRCh37 chr19: 23,621,430-24,071,154 , GRCh38.p12 chr19: 23,438,628-23,888,352	LOC100131479, LOC105372337, 13 more genes
nsv4372694	copy number variation	43	nstd173	human		GRCh37 chr6: 29,841,021-29,921,739 , GRCh38.p12 chr6: 29,873,244-29,953,962	HLA-A, MCCD1P1, 12 more genes
nsv4380209	copy number variation	18	nstd173	human		GRCh37 chr5: 103,506,757-103,537,589 , GRCh38.p12 chr5: 104,171,056-104,201,888	0
nsv4388385	copy number variation	148	nstd173	human		GRCh37 chr14: 106,537,003-106,560,975 , GRCh38.p12 chr: NaN-NaN	0

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